Rr695569 Other Genome Feature Detail

Summary

• Symbol
  Rr695569
• Name
  targeted mutation 695569
• Synonyms
  HS-39

• Feature Type
  CTCF binding site
• IDs
  MGI:8235454
• Regulates expression of
  Rhbdf1 (1 regulated gene)

Location &
Maps

• Sequence Map
  Genome coordinates not available from the current reference assembly.
• chr11:32187201-32187227 (GRCm39)

• Genetic Map
  Chromosome 11, Syntenic

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  3 phenotype references
  

• All Mutations and Alleles
  3
• Endonuclease-mediated
  2
• Targeted
  1
• Genomic Mutations
  1 involving Rr695569
• Find Mice (IMSR)
  0 strains or lines available

References

• Summaries
  All 4

  Phenotypes 3
• Earliest
  J:246278 Hanssen LLP, et al., Tissue-specific CTCF-cohesin-mediated chromatin architecture delimits enhancer interactions and function in vivo. Nat Cell Biol. 2017 Aug;19(8):952-961
• Latest
  J:366854 Kassouf MT, et al., The alpha-globin super-enhancer acts in an orientation-dependent manner. Nat Commun. 2025 Jan 25;16(1):1033

Rr695569 regulates expression of:

Feature	Feature Type	Location	Reference
Rhbdf1, rhomboid 5 homolog 1	protein coding gene	Chr11:32159585-32172300 (-)	J:246278